Publication Date

7-9-2018

Document Type

Article

Organizational Units

College of Natural Science and Mathematics, Biological Sciences, Physics and Astronomy

Keywords

Cell intercalation, Tricellular vertices, Oscillatory cycles, Asymmetric radial force

Abstract

Oriented cell intercalation is an essential developmental process that shapes tissue morphologies through the directional insertion of cells between their neighbors. Previous research has focused on properties of cell–cell interfaces, while the function of tricellular vertices has remained unaddressed. Here, we identify a highly novel mechanism in which vertices demonstrate independent sliding behaviors along cell peripheries to produce the topological deformations responsible for intercalation. Through systematic analysis, we find that the motion of vertices connected by contracting interfaces is not physically coupled, but instead possess strong radial coupling. E-cadherin and Myosin II exist in previously unstudied populations at cell vertices and undergo oscillatory cycles of accumulation and dispersion that are coordinated with changes in cell area. Additionally, peak enrichment of vertex E-cadherin/Myosin II coincides with interface length stabilization. Our results suggest a model in which asymmetric radial force balance directs the progressive, ratcheted motion of individual vertices to drive intercalation.

Copyright Date

7-9-2018

Copyright Statement / License for Reuse

Creative Commons Attribution 4.0 International License
This work is licensed under a Creative Commons Attribution 4.0 International License.

Rights Holder

The Authors

Provenance

Received from author

File Format

application/pdf

Language

English (eng)

Extent

23 pgs

File Size

5558 KB

Publication Statement

Copyright held by the authors. User is responsible for all copyright compliance. This article was originally published as:

Vanderleest, T. E., Smits, C. M., Xie, Y., Jewett, C. E., Blankenship, J. T., & Loerke, D. (2018). Vertex sliding drives intercalation by radial coupling of adhesion and actomyosin networks during Drosophila germband extension. eLife, 7, 1-23. DOI: 10.7554/elife.34586

Publication Title

eLife

Volume

7

First Page

1

Last Page

23

ISSN

2050-084X

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